Site Management Associate I
Core
Support clinical research projects by managing site communications, documents, and regulatory compliance.
Role type
Site Management Associate
Builds
Clinical trial operations and site readiness
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical research experience, regulatory knowledge, document management, inventory management, audit coordination, training coordination, English proficiency
Preferred skills
Administrative experience in international settings, MS Office proficiency
Technologies
CTMS, EDC, TMF, ISF
Responsibilities
Serve as main contact between site personnel and CRA for query resolution; Manage clinical supplies inventory and distribution; Ensure pre-study testing of site facilities; Coordinate regulatory and ethics committee submissions; Prepare for and follow up on site audits and inspections; Manage site-level Trial Master Files (TMF) and Investigator Site Files (ISF); Arrange project training for site teams.
Seniority
Entry-level to Junior
